ClinVar Miner

Submissions for variant NM_000365.6(TPI1):c.458-18del

gnomAD frequency: 0.00006  dbSNP: rs781911173
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002145667 SCV002451597 likely benign not provided 2023-11-04 criteria provided, single submitter clinical testing
Mayo Clinic Laboratories, Mayo Clinic RCV002145667 SCV002541519 uncertain significance not provided 2021-07-09 criteria provided, single submitter clinical testing

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